Maded Zeyad Khalaf, Lassoued Mohamed Ali, Taqa Ghada Abd Alrhman, Fawzi Hayder Adnan, Abdulqader Alaa Abdulelah, Jabir Majid S, Mahal Raffah Khamis, Sfar Souad
Laboratory of Pharmaceutical, Chemical, and Pharmacological Drug Development LR12ES09, Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Department of Dental Basic Sciences, College of Dentistry, University of Mosul, Mosul, Iraq.
Int J Nanomedicine. 2024 Dec 7;19:13113-13134. doi: 10.2147/IJN.S492180. eCollection 2024.
Phosphodiesterase-4 is an enzyme that regulates immune responses and contributes to the development of psoriasis. Dipyridamole and roflumilast function as phosphodiesterase-4 inhibitors, reducing pro-inflammatory cytokine expression. The aim was to evaluate the anti-psoriatic effect of the topical administration of dipyridamole and roflumilast nanoemulgel combination on imiquimod-induced psoriasiform skin inflammation in rats.
Dipyridamole and roflumilast were formulated into nanoemulgel to enhance skin penetration and retention. The production of nanoemulgels involves a two-part process. A nanoemulsion is created (the aqueous phase titration method was employed to create nanoemulsions), which is then incorporated into the gelling agent during the second phase. The new formula was then tested in rats. The rats were divided into seven groups; all animals were treated for 16 days. Induction was achieved by 120 mg of 5% imiquimod cream, which was applied daily for 8 days. After induction, groups received one of the following: 0.05% clobetasol ointment, 1% dipyridamole nanoemulgel (D-NEG), 0.3% roflumilast nanoemulgel (R-NEG), 1% dipyridamole and 0.3% roflumilast gel combination (DR-gel), and 1% dipyridamole and 0.3% roflumilast nanoemulgel combination (DR-NEG). At the end of the experiment, all animals were euthanized, and their blood and skin tissue samples were obtained. Inflammatory markers, immunohistochemistry, and histopathology were measured.
The DR-NEG group showed significantly lower levels of IL17, IL23, and TNF-α, while TGF-β showed higher levels than the clobetasol group. The expression of CK16 was significantly lower compared to the clobetasol group. DR-NEG showed a significantly lower PASI and Baker score than the clobetasol group.
The new DR-NEG's topical combination administration showed better anti-inflammatory, tissue healing, and anti-psoriatic activity than each drug alone or topical clobetasol administration; this could be attributed to the possible synergic effects of both drugs and the enhanced skin penetration offered by the nanoemulgel formulation.
磷酸二酯酶-4是一种调节免疫反应并参与银屑病发展的酶。双嘧达莫和罗氟司特作为磷酸二酯酶-4抑制剂,可减少促炎细胞因子的表达。本研究旨在评估双嘧达莫和罗氟司特纳米乳凝胶联合局部给药对咪喹莫特诱导的大鼠银屑病样皮肤炎症的抗银屑病作用。
将双嘧达莫和罗氟司特制成纳米乳凝胶以增强皮肤渗透和滞留。纳米乳凝胶的制备涉及两个步骤。首先制备纳米乳液(采用水相滴定法制备纳米乳液),然后在第二步中将其加入到胶凝剂中。然后在大鼠中对新配方进行测试。将大鼠分为七组;所有动物均接受16天的治疗。通过每日涂抹120mg 5%咪喹莫特乳膏,持续8天来诱导银屑病。诱导后,各组接受以下治疗之一:0.05%氯倍他索软膏、1%双嘧达莫纳米乳凝胶(D-NEG)、0.3%罗氟司特纳米乳凝胶(R-NEG)、1%双嘧达莫和0.3%罗氟司特凝胶组合(DR-凝胶)以及1%双嘧达莫和0.3%罗氟司特纳米乳凝胶组合(DR-NEG)。实验结束时,对所有动物实施安乐死,并获取其血液和皮肤组织样本。检测炎症标志物、进行免疫组织化学和组织病理学检查。
DR-NEG组的IL17、IL23和TNF-α水平显著降低,而TGF-β水平高于氯倍他索组。与氯倍他索组相比,CK16的表达显著降低。DR-NEG的银屑病面积和严重程度指数(PASI)和贝克评分显著低于氯倍他索组。
新的DR-NEG局部联合给药显示出比单独使用每种药物或局部使用氯倍他索更好的抗炎、组织愈合和抗银屑病活性;这可能归因于两种药物的协同作用以及纳米乳凝胶制剂增强的皮肤渗透性。